Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Gorlin syndrome (gene panel)	PTCH1, PTCH2, SUFU	Gorlin syndrome (3 genes)	Gorlin syndrome	Centre de Génétique Médicale UCL
Medulloblastoma (gene panel)	SUFU, TP53, PTCH1	Medulloblastoma (3 genes) - KUL	Medulloblastoma	Centrum Menselijke Erfelijkheid - KUL
Medulloblastoma (3 genes)	PTCH1, PTCH2, SUFU	Medulloblastoma (3 genes) - UCL	Medulloblastoma , Gorlin syndrome	Centre de Génétique Médicale UCL
MODY : Maturity onset Diabete of the Young (gene panel)	ABCC8, GCK, HNF1A, HNF4A, HNF1B, INS, KCNJ11	MODY - Maturity onset Diabete of the Young (21 genes) - IPG	MODY	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Canavan disease (hot spot mutation - p.Glu285Ala, p.Tyr231*)	ASPA		Mild Canavan disease, Severe Canavan disease	Centrum Medische Genetica - UZ Antwerpen
Jewish mutation panel (Tay Sachs, Fanconi, Dysautonomia, Canavan) (4 genes; 7 hot spot mutations)	ASPA, ELP1, HEXA, FANCC	Hot spot mutation among Jewish (4 genes, 7 mutations) - UZA		Centrum Medische Genetica - UZ Antwerpen
Ocular albinism and oculocutaneous albinism type 1, 2, 3, 4, 6, 7, 8 (gene panel)	TYR, OCA2, TYRP1, SLC45A2, SLC24A5, LRMDA, GPR143	Ocular and oculocutaneous albinism - UGent	Oculocutaneous albinism type 1A, Oculocutaneous albinism type 1B, Oculocutaneous albinism type 2, Oculocutaneous albinism type 3, Oculocutaneous albinism type 4, Oculocutaneous albinism type 6, Oculocutaneous albinism type 7	Centrum Medische Genetica - UZ Gent

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